Canonical Allele Identifier: PA2826093131
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 4923

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165401.1:p.Asp1341Asn
CA253334
NM_001171930.2:c.4021G>A